Allele Registry

Canonical Allele Identifier: PA275665

Gene: AGXT HGNC NCBI

ClinVar RCV:

RCV000186295

ClinVar Variation:

204089

HGVS (amino-acid)	Matching Registered Transcripts
NP_000021.1:p.Trp108Cys	CA275664 NM_000030.3:c.324G>T CA351313855 NM_000030.3:c.324G>C